T Butyl 2 4 Pyridine 2 Yl Benzyl Hydrazinecarboxylate
pyridine pyrrole pyrazine piperidine piperazine

t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate

    Specifications

    HS Code

    886546

    Chemical Formula C21H26N4O2
    Molecular Weight 366.46 g/mol
    Appearance Solid (usually)
    Solubility In Water Low (organic compound, likely hydrophobic)
    Solubility In Organic Solvents Moderate to high in common organic solvents like dichloromethane, chloroform
    Stability Stable under normal conditions but may react with strong oxidizing or reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading t-butyl-2-(4-(pyridine-2-yl)benzyl)hydrazinecarboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of the T-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazinecarboxylate?
    Eh! The chemical structure of t - butyl - 2 - (4- (pyridine - 2 - yl) benzyl) hydrazinecarboxylate. The name of this compound is composed of several parts. "T - butyl", tert - butyl also, its structure is a carbon atom with three methyl groups, in the shape of an umbrella. "hydrazinecarboxylate", is a hydrazine carboxylic acid ester group, containing the structure of hydrazine (- NH - NH) and carboxylic acid esters, that is - NH - NH - COO -.
    As for "2- (4- (pyridine - 2 - yl) benzyl) ", "benzyl" is benzyl, that is, benzyl, and benzyl cyclic monomethylene (-CH -2 -). "4- (pyridine - 2 - yl) " indicates that the para-position (4-position) of benzyl is connected to pyridine - 2 - group, pyridine is a nitrogen-containing six-membered heterocyclic ring, and 2 - group refers to the carbon in the adjacent position of the nitrogen atom that is connected to the para-position of benzyl.
    In summary, this compound is connected to the nitrogen atom of hydrazine carboxylate with tert-butyl group, and the nitrogen atom on the other side of the ester group is connected with benzyl group containing specific substituent group, and benzyl group is connected to pyridine-2 -group. This structure fuses aromatic rings, heterocycles and functional groups containing nitrogen and oxygen, and has a delicate structure. It may have unique properties and uses in the research and application of organic chemistry.
    What are the main uses of T-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazinecarboxylate?
    Tert-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazine carboxylate, a compound in the field of organic chemistry. It has a wide range of uses in the field of medicinal chemistry and is often used as a key intermediate for the synthesis of drug molecules with specific biological activities. Geinpyridine and benzyl structures can endow drugs with specific spatial configurations and electronic properties, or can enhance the affinity and selectivity of drugs to specific targets, laying the foundation for the development of new drugs.
    In the field of materials science, this compound may be introduced into the structure of polymer materials through specific chemical reactions. With its unique chemical structure, it can improve the physical and chemical properties of materials such as solubility, thermal stability, mechanical properties, etc., and then expand the application of materials in special fields.
    In the field of pesticide chemistry, or due to the special structure of the compound, it shows inhibitory or killing activity against certain pests or pathogens. After reasonable modification and optimization, it is expected to be developed into a new type of pesticide to help agricultural pest control. With its unique chemical structure, this compound has potential application value in many fields. It is like a good material in the hands of ancient skilled craftsmen. It can be carved into various exquisite utensils, contributing to the development of different fields.
    What are the synthesis methods of t-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazinecarboxylate?
    To prepare t - butyl - 2 - (4 - (pyridine - 2 - yl) benzyl) hydrazinecarboxylate, there are many methods. First, 4 - (pyridine - 2 - yl) benzyl halide can be reacted with tert-butyl hydrazinocarboxylate under the action of alkali. For bases, such as potassium carbonate, sodium carbonate, etc., in suitable organic solvents, such as acetonitrile, N, N - dimethylformamide, etc., heated and stirred to obtain the product.
    Second, an amine compound containing pyridine - 2 - yl benzyl is first prepared, and then reacted with tert-butyl chloroformate. Amine compounds can be reacted with tert-butyl chloroformate in an alkaline environment, such as triethylamine, and in an organic solvent such as dichloromethane to obtain the target product.
    Or, using 4 - (pyridine - 2 - yl) benzoic acid as the starting material, first convert it into an acid chloride, and then react with tert-butyl hydrazine. The preparation of acid chloride can be achieved by reagents such as oxalyl chloride and dichlorosulfoxide in a suitable solvent such as dichloromethane, and then react with tert-butyl hydrazine in the presence of a base. The purpose of synthesis can also be achieved through this step.
    All methods have advantages and disadvantages. In actual operation, when considering the availability of raw materials, the difficulty of reaction conditions, the purity of the product and other factors, select the best one and use it to achieve high efficiency and high quality synthesis of t - butyl - 2 - (4 - (pyridine - 2 - yl) benzyl) hydrazinecarboxylate purpose.
    What are the physical properties of t-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazinecarboxylate?
    Alas! This t - butyl - 2 - (4 - (pyridine - 2 - yl) benzyl) hydrazinecarboxylate is also an organic compound. Its physical properties are quite important. Looking at its shape, under normal conditions, it may be a white to white solid, just like the white snow, pure and delicate. This is because its molecular structure is arranged in an orderly manner and the interaction is stable, so it appears as a solid state.
    When talking about the melting point, it is about a specific temperature range, just like that everything has a certain number, and its melting point is its inherent property. When heated, the molecule is energized, the vibration intensifies, the lattice structure gradually loosens, and finally the melting point, the solid state turns into a liquid state, just like the melting of ice and snow.
    In addition to solubility, in organic solvents, such as dichloromethane, ethanol, etc., there may be a certain solubility. This is due to the principle of "similar miscibility", and there is a suitable force between its molecular structure and the molecules of the organic solvent, which can blend with each other. However, in water, the solubility may be very small, because the polarity of the molecule and the polarity of the water molecule are quite different, and it is difficult to miscible with each other, just like the mutual exclusion of oil and water.
    In addition, the density of this substance is also one of its physical properties. Although the value is specific, the density is important when it interacts with surrounding substances. If it participates in the reaction, the density affects its distribution in the system, which in turn affects the reaction process. If it is like marching into battle, each in its place can win thousands of miles. < Br >
    Its refractive index is also of symbolic significance. When light passes through this object, due to the action of molecules on light, the refraction angle has a specific value, which can help to identify its purity and structure, just like reading the "code" of light, explaining the mystery of molecules.
    What are the chemical properties of T-butyl-2- (4- (pyridine-2-yl) benzyl) hydrazinecarboxylate?
    Eh, this t - butyl - 2 - (4 - (pyridine - 2 - yl) benzyl) hydrazinecarboxylate is an organic compound. It has unique chemical properties.
    Looking at its structure, it contains tert-butyl, benzyl, pyridyl and hydrazine groups. This structure makes its properties quite different. In terms of physical properties, due to the large tert-butyl group, the molecule has a certain spatial resistance, or affects its solubility in solvents. Usually, in organic solvents such as dichloromethane, chloroform, etc., or have good solubility, but in water, because of its dominant hydrophobic groups, solubility is not good.
    In terms of chemical properties, hydrazine carboxylate is partially reactive. The hydrogen on its nitrogen atom can participate in nucleophilic reactions, such as condensation with aldose and ketone to form hydrazone compounds. Pyridyl groups are basic aromatic heterocycles, which can form salts with acids, and can also participate in metal-catalyzed coupling reactions, such as Suzuki coupling, Buchwald-Hartwig coupling, etc., to construct more complex organic structures. The benzyl part of the benzyl ring can undergo electrophilic substitution reactions, such as halogenation, nitrification, etc., while the hydrogen on benzyl carbons also has certain activity and can be oxidized or replaced under appropriate conditions. In conclusion, this compound has many potential reaction paths and applications in the field of organic synthesis due to its unique structure.